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Page 1: Mr. Robert Perdue
Page 2: Mr. Robert Perdue

Mr. Robert Perdue Page 2 June 8, 2006 Enclosures: Form 200

Attachment 1 – Updated Narrative Project Description Attachment 2 – Updated Site Layout Drawing Attachment 3 – Updated Influent and Effluent Characteristics

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Form 200

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Attachment 1 Narrative Project Description

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Attachment 1 – Narrative Project Description

Pacific Gas and Electric Company (PG&E) is implementing an Interim Measure (IM) to address chromium in groundwater at the Topock Compressor Station under the oversight of the California Environmental Protection Agency, Department of Toxic Substances Control (DTSC). The IM consists of groundwater extraction in the Colorado River floodplain and management of extracted groundwater. The groundwater extraction, treatment, and injection systems are collectively referred to as Interim Measure No. 3 (IM No. 3). Currently, the IM No. 3 facilities include an existing groundwater extraction system, conveyance piping, a groundwater treatment plant, and an injection well field for the discharge of the treated groundwater.

On October 13, 2004, the California Regional Water Quality Control Board, Colorado River Basin Region (Water Board) adopted Waste Discharge Requirements (WDR) Order No. R7-2004-0103, which authorized PG&E to inject treated groundwater into an injection well field at the Topock site. The WDRs specify effluent limitations, prohibitions, specifications, and provisions for subsurface injection. Startup of the IM No. 3 treatment system occurred over a 3-day period from July 25 to July 27, 2005, in accordance with Order R7-2004-0103, and injection has been occurring in compliance with the Order requirements since that time.

Order R7-2004-0103 expires on January 31, 2007 (Provision D.23). To support PG&E’s Report of Waste Discharge renewal application, this narrative project description provides supplemental information on the subsurface injection of treated water.

The information contained in this narrative project description is very similar to that which was contained in the original Report of Waste Discharge for subsurface injection of treated water submitted to the Water Board on August 13, 2004. Information from the original application has been updated following the construction, start-up, and operation of the treatment and injection system to reflect current operating conditions. Subsequent to filing the original Report of Waste Discharge, and as required by Order R7-2004-0103, PG&E submitted additional information on the subsurface injection of treated water, as outlined in the documents in Table 1.

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TABLE 1 Documents Required by Order R7-2004-0103 and Associated Monitoring and Reporting Program (MRP)a

Document and Requirement of Order R7-2004-0103

Date Document Submitted to the Water Board

Injection System O&M Plan –Provision D.4

Submitted to Water Board and DTSC on April 7, 2005. Addendum 1 and Addendum 2 submitted June 3, 2005 and June 30, 2005, respectively.

Design Plan for Groundwater Compliance Monitoring - Provision D.6

Submitted to Water Board and DTSC on November 23, 2004. Incorporated agency comments and re-submitted to Water Board and DTSC on January 5, 2005.

Contingency Plan for any plant upset – Provision D.8

Submitted to Water Board on April 15, 2005 as part of Treatment System O&M Plan. Updated and re-submitted to Water Board on April 24, 2006.

Solid Waste Management Plan – Provision D.19

Submitted to Water Board on March 24, 2004. Clarification letter submitted on July 1, 2005.

Groundwater Compliance Monitoring Plan – MRP, Groundwater Monitoring 1

Submitted to Water Board and DTSC on April 11, 2005. Incorporated agency comments and re-submitted to Water Board and DTSC on June 17, 2005. Addendum to CMP submitted December 13, 2005.

Sampling Stations – MRP, Startup 2 Submitted to Water Board June 29, 2005

Startup Report – MRP, Startup 4 Submitted to Water Board August 12, 2005

a In addition to the documents listed in the table, PG&E has submitted the monitoring reports required by the MRP, in accordance with the required reporting frequency.

Facility Location As discussed above, the IM No. 3 system extracts groundwater, treats the groundwater, and discharges the treated water using subsurface injection wells. Extracted groundwater is conveyed by piping (influent) to the treatment system located on San Bernardino County Assessor’s Parcel No. 650-151-06. The treated water is conveyed by piping (effluent) to the injection wells, located at the west side of the Parcel 650-151-06. The site layout drawing showing the location of the IM No. 3 extraction, conveyance, treatment, and injection facilities is presented as Attachment 2.

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Treatment System Flow Rates The groundwater extraction and treatment system is designed to handle influent groundwater flows up to 135 gallons per minute. The treated effluent flow rate will be in the range of 80 to 95 percent of the influent flow. In addition, treatment residuals include:

• Reverse osmosis concentrate stream containing 18,000 to 24,000 milligrams per liter (mg/L) of total dissolved solids at a flow rate of 5 to 20 percent of influent flow.

• Precipitated solids at a concentration of up to 30 percent solids. The volume of solids varies with treatment conditions, but it is on the order of 100 pounds (dry weight) per day.

Influent and Treated Discharge Characteristics Influent groundwater and treated effluent characteristics are presented in Attachment 3. The treatment system removes chemically-reduced and precipitated chromium as well as total dissolved solids. Current effluent limitations as stated in the WDR Order No. R7-2004-0103 are shown in Table 2 below

TABLE 2 Effluent Limitations for Chromium (VI) and Chromium (Total) in Order R7-2004-0103

Constituent Unit Average Monthly Effluent Limit

Maximum Daily Effluent Limit

Chromium (VI) µg/L 8 16

Chromium (Total) µg/L 25 50

In addition, the pH of the effluent is to be maintained within the limits of 6.5 to 8.4, and the effluent is not to contain heavy metals, chemicals, pesticides or other constituents in concentrations toxic to a human health.

The average total dissolved solids concentration in the treated effluent is currently controlled to target 4,200 mg/L, based on the representative total dissolved solids value for the injection area groundwater (Groundwater and Hydrogeologic Investigation Report for Interim Measures No. 3 Injection Area, CH2M HILL, June 2005).

Treatment System Description The treatment system includes chemical reduction of hexavalent chromium to trivalent chromium, precipitation and settling of the resulting insoluble chromium hydroxide, microfiltration to remove remaining suspended particulate matter, and reverse osmosis to remove dissolved salts. The groundwater entering the treatment system may be classified as a hazardous waste (chromium concentrations equal to or greater than 5 mg/L) under

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California hazardous waste regulations. Consequently, the treatment system was permitted through the California Tiered Permitting Program under the jurisdiction of the San Bernardino Fire Department, Hazmat Division, which is the Certified Unified Program Agency for San Bernardino County.

The reagents used for treatment of the groundwater include ferrous chloride (for chromium removal), sulfuric acid (for pH control), sodium hydroxide (for pH control to improve precipitation), an anionic polymer to facilitate particle settling, and an anti-scalant to reduce mineral buildup on reverse osmosis membrane surfaces. Reagents are stored and handled in compliance with applicable federal, state, and local requirements.

Ferrous chloride is injected into influent groundwater within a recycle loop pipe reactor, along with sulfuric acid, if required for pH control. The pH setpoint range is from 4.5 to 6.8 and the ferrous chloride dose range is from 45 to 200 mg/L depending on the influent hexavalent chromium concentration. The pipe reactor converts hexavalent chromium to trivalent chromium. Next, the water flows through a chromium reduction tank reactor to ensure complete conversion of remaining hexavalent chromium to trivalent chromium.

The treated groundwater then flows through three oxidation tanks in series. Air is bubbled through these tanks to oxidize soluble ferrous iron to the very insoluble ferric form. The resulting ferric hydroxide precipitate co-precipitates trivalent chromium hydroxide to remove it from the groundwater. Sodium hydroxide is added to one or more of the three tanks to raise the pH of the groundwater to the range 7.5 to 8.2 to further promote precipitation of iron and trivalent chromium.

Treated groundwater from the three tanks flows into an inclined plate clarifier. Sludge drops to the bottom, thickening section of the clarifier, where it is transferred into a container for temporary storage prior to discharge to a container for offsite disposal. Treated wastewater exiting the clarifier is further treated in a microfilter. Solids rejected by the microfilter are returned to the raw water tank. A portion of the microfilter-treated effluent is treated in a reverse osmosis system.

The reverse osmosis system removes and concentrates soluble salts. Total dissolved solids concentrations of water entering the reverse osmosis system are reduced from a range of 5,000 to 8,000 mg/L (based on the blend of Extraction Wells TW-2D, TW-3D, and PE-1), which is lowered to 500 to 1,000 mg/L by the reverse osmosis system. The reverse osmosis permeate is blended with that portion of the microfiltered water that has bypassed the reverse osmosis system to achieve the target effluent total dissolved solids concentration specified in Order R7-2004-0103. Treated water is piped to one or both of the two injection well sites in single-contained piping following the piping alignment shown in Attachment 2.

The reverse osmosis concentrate has an estimated total dissolved solids concentration of 18,000 to 32,000 mg/L. It is conveyed from the treatment system to the MW-20 bench using the same trench as for the influent piping. Storage facilities are located at the MW-20 bench to accommodate the reverse osmosis concentrate stream. The reverse osmosis concentrate is trucked to an offsite permitted disposal facility.

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Treatment Chemical Usage Treatment chemicals and estimated usage rates are:

• Thirty-five percent solution of ferrous chloride: 80 to 140 gallons per day.

• Thirty-five percent solution of sulfuric acid: not required by current groundwater chemistry.

• Twenty-five percent solution of sodium hydroxide: 5 gallons per day.

• Anti-scalant: 2.6 gallons per day.

• Anionic polymer to facilitate floc formation and solids removal in clarifier: approximately 1 pound per day.

Best Management Practices The following best management practices are in place to prevent releases of hazardous materials or untreated groundwater:

• Treatment chemicals are brought to the site in totes or smaller containers. They are stored and used in a secondarily-contained area.

• The influent groundwater tank and the treatment system are constructed on a coated concrete treatment pad with curbing to contain drips and spills. Groundwater influent to the treatment plant is conveyed in secondary containment piping with electronic leak detection.

• Hazardous materials usage is governed by a Hazardous Materials Business Plan that specifies the location of hazardous materials onsite and includes a spill contingency and emergency response plan.

• Hazardous wastes are managed in accordance with the requirements of Title 22, California Code of Regulations, Division 4.5.

• A treatment system operations manual is maintained at the site. System operators are trained regarding system operation, maintenance, and emergency procedures.

• Electronic control loops are included in the system design to link extraction well operations with treatment system operations; regulate process flow rates within the plant; discharge the treated water and wastes; flow-pace chemical feeds; and backwash filters.

• Level alarms/switches are provided in tanks to prevent overflows and damage to pumps.

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• The pH and key flow rates are continuously monitored to assess plant performance. Filter effluent turbidity and periodic analytical tests are used to monitor treatment process performance.

• Extraction well pumps and plant operations are shut down in the event of a process failure and/or mechanical damage. Alarms are indicated on a local control panel at the treatment unit. A manual reset is required to restart the plant.

• Monitoring of treatment plant performance includes online monitoring of pH, key flow rates, and filter effluent turbidity, as well as periodic effluent sampling and analysis. Testing of effluent, influent, reverse osmosis concentrate, and sludge solids is done per the requirements of Order R7-2004-0103 and the associated Monitoring and Reporting Program.

Disposal of Treatment Residuals The precipitated solids removed in the clarifier and the reverse osmosis concentrate are trucked offsite to permitted disposal facilities in accordance with federal, state, and local regulations.

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Attachment 2 Site Layout Drawing

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MW-37SMW-37D

MW-34-080MW-34-55

MW-33-90MW-33-40

MW-32-35MW-32-20

MW-30-50MW-30-30

MW-28-90MW-28-25

MW-35-135MW-35-060

MW-31-135MW-31-060

MW-20-130MW-20-100

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BAO \\ZINFANDEL\PROJ\PACIFICGASELECTRICCO\TOPOCKPROGRAM\GIS\MXD\2006\IM3_PROJECT_AREA_MAY06.MXD IM3_PROJECT_AREA_MAY06.PDF 5/8/2006 15:35:02

FIGURE 1IM-3 FACILITIES AND GENERAL SITE FEATURESIM-3 COMPLIANCE MONITORING PROGRAMPG&E TOPOCK COMPRESSOR STATIONNEEDLES, CALIFORNIA

California State Plane NAD83 Zone 5 US Feet

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Attachment 3 Updated Influent and Effluent Characteristics

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Attachment 3Influent Groundwater and Treated Effluent CharacteristicsPG&E Topock Interim Measures No. 3

AnalyteAverage

Frequency of Detection

UnitsGroupInfluent

Frequency of Detection

Effluent

MaxDate of

MaxAverage MaxDate of

Max

Actual Data Collected During Operations August 2005 to April 2006Original ROWD Submittal

Influent Effluent

Average Max Average Max

a

c, d c, d c c

b

3.3613 / 13mg/LNitrate as NitrogenANION 13 / 13 4.18 12/13/20054.69 5.69 8/29/2005--- --- --- ---0.008228 / 9mg/LNitrite as Nitrogen 7 / 9 0.0211 8/16/20050.00878 0.0143 8/16/2005--- --- --- ---

---0 / 0mg/LBromide 0 / 0 --- ------ --- ---2.7 5.2 ND (0.5) ND (0.5)1.9113 / 13mg/LFluoride 13 / 13 2.31 12/7/20052.54 3.07 8/16/20050.8 1.5 ND (2) ND (2)45013 / 13mg/LSulfate 13 / 13 528 2/1/2006691 742 2/1/20061117 5510 17 82.65

681024 / 24µS/cmSpecific conductanceGeneral 44 / 44 8530 3/29/20069290 11000 2/1/2006--- --- --- ---0.06569 / 24NTUTurbidity 6 / 44 0.256 8/4/20050.0834 0.219 9/21/2005--- --- --- ---

NA1 / 10mg/LTotal organic carbon 0 / 9 ND (0.3) NA0.32 1.25 4/5/20066.2 39 0.9 5.8NA0 / 10mg/LTotal suspended solids 0 / 10 ND (10) NANA ND (10) NA3.9 5.6 ND (2) ND (2)

399024 / 24mg/LTotal dissolved solids 57 / 57 4810 12/7/20055890 6360 9/21/200511296 43,600 500 1000e

1.473 / 9mg/LAmmonia as nitrogen 4 / 9 7.84 11/2/20050.509 1.43 10/12/20052.0 12.3 0.20 1.2ffgpmFlow f 121.4 Feb 2006f 134.1 Feb 200680 135 80 135

---0 / 0deg FWinter Temperature 0 / 0 --- ------ --- ---55 60 55 60---0 / 0deg FSummer Temperature 0 / 0 --- ------ --- ---80 85 80 85

7.8824 / 24phunitspH 44 / 44 8.14 2/8/20067.51 7.72 9/28/20057.5 7.9 6.2 70.1398 / 11mg/LTotal phosphorus as p 10 / 10 0.258 8/8/20050.054 0.219 8/1/20050.18 0.25 ND (0.05) ND (0.05)

---0 / 0mg/LSulfide 0 / 0 --- ------ --- ---ND (0.4) 0.7 ND (0.4) ND (0.4)

0.00044124 / 24mg/LHexavalent chromiumMetals - Filtered 12 / 44 0.00046 8/16/20053.77 4.27 8/25/20054.9 8.3 ND (0.010) ND (0.010) g

NA0 / 13mg/LAntimonyMetals-Unfiltered 0 / 13 ND (0.003) NANA ND (0.003) NA--- --- --- ---NA0 / 13mg/LArsenic 0 / 13 ND (0.005) NANA ND (0.005) NA--- --- --- ---NA0 / 12mg/LAluminum 0 / 12 ND (0.052) NANA ND (0.052) NAND (0.05) ND (0.05) ND (0.05) ND (0.05)

0.09226 / 13mg/LBarium 6 / 13 0.104 8/1/20050.0919 0.027 9/16/20050.3 1.1 ND (0.025) ND (0.025)h

1.3313 / 13mg/LBoron 13 / 13 1.62 11/2/20051.40 1.66 3/8/20061.9 3.6 0.750 1.44NA0 / 12mg/LIron 0 / 12 ND (0.3) NANA ND (0.3) NA0.78 9.3 ND (0.1) ND (0.1)

11.15 / 5mg/LMagnesium 5 / 5 14.7 8/22/200521.4 23.2 8/29/2005175 985 5 29.550.0088513 / 13mg/LMolybdenum 12 / 13 0.0122 12/7/20050.0212 0.028 8/22/20050.03 0.1 0.003 0.010

NA0 / 13mg/LManganese 0 / 13 ND (0.05) NANA ND (0.05) NA0.24 1.3 0.007 0.0390.0010624 / 24mg/LChromium 5 / 44 0.0107 1/18/20064.05 7.14 8/4/20055.4 10.4 ND (0.025) ND (0.025)0.001241 / 13mg/LLead 1 / 13 0.0024 3/8/20060.00124 0.0024 3/8/20060.03 0.073 0.0004 0.0010.007355 / 13mg/LNickel 2 / 13 0.0093 9/16/20050.00818 0.0079 8/16/20050.04 0.5 0.004 0.050.05818 / 13mg/LZinc 8 / 13 0.406 4/5/20060.039 0.197 4/5/20060.09 0.6 0.003 0.018

0.014 / 13mg/LCopper 5 / 13 0.0328 3/8/20060.0101 0.0313 3/8/20060.02 0.2 0.002 0.016

---0 / 0unitsColorOTHER 0 / 0 --- ------ --- ---143 150 --- ---

NOTES:

Assessment based on existing data prior to July 2004 from wells TW-2S, TW-2D, MW-26, MW-30-30.

For nondetect results, a value equal to half the reporting limit is used to calculate average concentration from each sample. Sometimes the reporting limit may be higher than the detected value causing the average to be higher than the maximum value.

Average concentrations are flow-weighted assuming flow from wells TW-2S, TW-2D, MW-26, MW-30-30, with 50% from TW-2D and 16.6% each from the other wells.

Assessment based on existing data between August 2005 and April 2006 from influent and effluent sampling locations SC-100B and SC-700B.

a

c

d

b

Flow is measured continuously and reported as a monthly averagef

mg/LµS/cmNTUdeg FgpmND---NA

milligrams per litermicrosiemens per centimeter nephelometric turbidity unitsdegree fahrenheitgallons per minuteparameter not detected at the listed reporting limitnot samplednot applicable because all samples are not detected

The maximum value was detected during two events.

Reporting limit increased from 0.003 mg/L to 0.3 mg/L for all analyses completed after September 2005.h

g

e Subsequent to original ROWD submittal, PG&E and the Water Board agreed on approach to estalish and monitor TDS so that discharge is consistant with the Anti-Degradation Policy.

G:\PacificGasElectricCo\TopockProgram\Database\Tuesdai\IM3WDR\PurgeWater\TopockStatsRev2.mdb\rpt_InfEff_Stats4 Date Printed: 5/24/2006Page 1 of 1